EP1776190A1 - Plug-flow regeneration process - Google Patents
Plug-flow regeneration processInfo
- Publication number
- EP1776190A1 EP1776190A1 EP05764193A EP05764193A EP1776190A1 EP 1776190 A1 EP1776190 A1 EP 1776190A1 EP 05764193 A EP05764193 A EP 05764193A EP 05764193 A EP05764193 A EP 05764193A EP 1776190 A1 EP1776190 A1 EP 1776190A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- resin
- stage
- vessel
- regenerant
- regeneration
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000008929 regeneration Effects 0.000 title claims abstract description 361
- 238000011069 regeneration method Methods 0.000 title claims abstract description 361
- 238000000034 method Methods 0.000 title claims abstract description 241
- 230000008569 process Effects 0.000 title claims abstract description 222
- 239000011347 resin Substances 0.000 claims abstract description 636
- 229920005989 resin Polymers 0.000 claims abstract description 636
- 239000012492 regenerant Substances 0.000 claims abstract description 346
- 239000003456 ion exchange resin Substances 0.000 claims abstract description 57
- 229920003303 ion-exchange polymer Polymers 0.000 claims abstract description 57
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims abstract description 38
- 238000011049 filling Methods 0.000 claims abstract description 37
- 230000001172 regenerating effect Effects 0.000 claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 205
- 239000012530 fluid Substances 0.000 claims description 109
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical group O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims description 93
- 239000012267 brine Substances 0.000 claims description 77
- 238000003860 storage Methods 0.000 claims description 39
- 239000000243 solution Substances 0.000 claims description 36
- 239000002699 waste material Substances 0.000 claims description 34
- 238000005342 ion exchange Methods 0.000 claims description 32
- 238000002791 soaking Methods 0.000 claims description 15
- 150000002500 ions Chemical class 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000012141 concentrate Substances 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000006249 magnetic particle Substances 0.000 claims description 6
- 238000001179 sorption measurement Methods 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 229910002651 NO3 Inorganic materials 0.000 claims description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 229910001422 barium ion Inorganic materials 0.000 claims description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- 229910001430 chromium ion Inorganic materials 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 2
- 238000012546 transfer Methods 0.000 description 65
- 150000003839 salts Chemical class 0.000 description 19
- 239000002245 particle Substances 0.000 description 18
- 238000012545 processing Methods 0.000 description 15
- 230000008901 benefit Effects 0.000 description 14
- 238000009826 distribution Methods 0.000 description 13
- 239000011324 bead Substances 0.000 description 12
- 238000010586 diagram Methods 0.000 description 12
- 239000003651 drinking water Substances 0.000 description 12
- 230000005484 gravity Effects 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 12
- 239000012528 membrane Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 235000012206 bottled water Nutrition 0.000 description 10
- 238000013461 design Methods 0.000 description 10
- 238000007792 addition Methods 0.000 description 9
- 238000005374 membrane filtration Methods 0.000 description 9
- 239000012508 resin bead Substances 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 230000003204 osmotic effect Effects 0.000 description 8
- 238000005086 pumping Methods 0.000 description 8
- 230000035939 shock Effects 0.000 description 8
- 239000000701 coagulant Substances 0.000 description 7
- 238000012423 maintenance Methods 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000005345 coagulation Methods 0.000 description 6
- 230000015271 coagulation Effects 0.000 description 6
- 229910003460 diamond Inorganic materials 0.000 description 6
- 239000010432 diamond Substances 0.000 description 6
- 239000013505 freshwater Substances 0.000 description 6
- 230000006870 function Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 125000002091 cationic group Chemical group 0.000 description 5
- 150000003841 chloride salts Chemical class 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 239000003792 electrolyte Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- 235000015598 salt intake Nutrition 0.000 description 5
- 239000012266 salt solution Substances 0.000 description 5
- 238000004659 sterilization and disinfection Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000000645 desinfectant Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 239000004021 humic acid Substances 0.000 description 4
- 238000004062 sedimentation Methods 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 229910052770 Uranium Inorganic materials 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000005352 clarification Methods 0.000 description 3
- 239000002509 fulvic acid Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000009434 installation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000009428 plumbing Methods 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 238000012384 transportation and delivery Methods 0.000 description 3
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 3
- -1 uranyl ions Chemical class 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229940037003 alum Drugs 0.000 description 2
- 239000001164 aluminium sulphate Substances 0.000 description 2
- 235000011128 aluminium sulphate Nutrition 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000005115 demineralization Methods 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000008235 industrial water Substances 0.000 description 2
- 159000000014 iron salts Chemical class 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000001728 nano-filtration Methods 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 238000001223 reverse osmosis Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000010865 sewage Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 description 1
- QDHHCQZDFGDHMP-UHFFFAOYSA-N Chloramine Chemical class ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004155 Chlorine dioxide Substances 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000019398 chlorine dioxide Nutrition 0.000 description 1
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 125000004122 cyclic group Chemical class 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000003673 groundwater Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 238000007726 management method Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000001471 micro-filtration Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 238000006385 ozonation reaction Methods 0.000 description 1
- 238000003921 particle size analysis Methods 0.000 description 1
- 238000007415 particle size distribution analysis Methods 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000005067 remediation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 238000004148 unit process Methods 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J49/00—Regeneration or reactivation of ion-exchangers; Apparatus therefor
- B01J49/05—Regeneration or reactivation of ion-exchangers; Apparatus therefor of fixed beds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J49/00—Regeneration or reactivation of ion-exchangers; Apparatus therefor
- B01J49/50—Regeneration or reactivation of ion-exchangers; Apparatus therefor characterised by the regeneration reagents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/16—Regeneration of sorbents, filters
Definitions
- the present invention relates to water treatment, and in particular to water treatment processes which involve the use of ion-exchange resins.
- the invention relates to a process for regenerating ion-exchange resin used in such processes.
- a coagulant is applied to destabilise and combine with suspended matter and DOC so that they coalesce and form a floe, which can then be physically removed by methods such as floating, settling, filtration or a combination thereof.
- Coagulants such as alum (aluminium sulphate), various iron salts and synthetic polymers are commonly used in processes for water treatment.
- DOC aluminium sulphate
- many raw water sources have high levels of DOC present, which reacts with the coagulant requiring a higher coagulant dose than would be required for removal of suspended matter alone.
- the treated water may contain as much as 30-70% of the initial
- MF Microfiltration
- UF Ultrafiltration
- NF Nanofiltration
- RO Reverse Osmosis
- Ion-exchange resins can also be used for removing DOC present in raw water.
- Ion- exchange techniques conventionally involve passing water through a packed bed or column of ion-exchange resin.
- Target species such as DOC are removed by being adsorbed onto the ion-exchange resin.
- Ion-exchange resins have been used to remove up to 90% of the DOC in raw water.
- Ion-exchange resins may also be used in conjunction with other methods of water purification including those mentioned previously. Sufficient resin may be added to remove a percentage of the DOC such that the cost of any subsequent treatment used to meet water quality objectives is minimised. For example, the use of ion-exchange resin for the removal of DOC can facilitate the reduction of the amount of coagulant required to achieve acceptable product water quality. Ion-exchange resin may also aid in significantly reducing the capital and operating costs of membrane filtration.
- the ion-exchange resins should be recyclable and regenerable. Recyclable resins can be used multiple times without regeneration and continue to be effective in adsorbing DOC. Regenerable resins are capable of being treated to remove adsorbed DOC, and as such, these regenerated resins can be reintroduced into the treatment process.
- Ion-exchange resins incorporating dispersed magnetic particles readily agglomerate due to the magnetic attractive forces between them. This property renders them particularly useful as recyclable resins as the agglomerated particles tend to settle quickly and are therefore more readily removable from the water.
- a particularly useful magnetic ion-exchange resin for the treatment of raw water is described in WO96/07675, the entire contents of which is incorporated herein by reference.
- the resin disclosed in this document has magnetic particles dispersed throughout the polymeric beads such that even when the resin become worn through repeated use, the worn resin retains the magnetic character.
- Ion exchange beads of the type disclosed in this document are available from Orica Australia Pty. Ltd., under the trademark, MIEX ® .
- MIEX ® One of the benefits of using MIEX ® resin is that its small size allows the resin to be pumped.
- WO 96/07615 describes a process for removing DOC from water using an ion-exchange resin which can be recycled and regenerated. This process is particularly useful in treating raw water with magnetic ion-exchange resin of the type described in WO96/07675.
- the preferred ion-exchange resins disclosed in WO96/07675 are magnetic ion-exchange resins which have, throughout their structure, cationic functional groups which provide suitable sites for the adsorption of DOC. These cationic functional groups possess negatively charged counter-ions which are capable of exchanging with the negatively charged DOC.
- the negatively charged DOC is removed from the raw water through exchange with the resin's negative counter ion.
- DOC becomes bound to the magnetic ion-exchange resin and the function of the ion-exchange resin is reduced.
- Such resins can be referred to as used, spent or loaded resins.
- When producing potable water for distribution and consumption it is particularly important to be able to regenerate the loaded resin in an efficient and cost-effective manner. This can also be important when using ion-exchange resins for other purposes such as removal of contaminants in potable or waste water treatment and metal recovery.
- WO 96/07615 discloses a process for regenerating magnetic ion-exchange resin by contacting it with brine (which is substantially a NaCl solution).
- brine which is substantially a NaCl solution.
- the brine solution in such a process is the "regenerant”.
- the resin is regenerated by the exchange of a chloride ion for a DOC ion from the loaded resin.
- the byproduct from regeneration is referred to as the "spent regenerant” and is primarily a mixture of the removed DOC and brine.
- the spent regenerant from a regeneration process is discharged into the ocean or may be used as land fill.
- the regeneration process disclosed in WO 96/07615 involves passing brine through a packed column of loaded resin.
- the regeneration can also be affected by a mixing or agitation process.
- these regeneration processes are performed in large batch wise operations. For example, loaded MIEX ® resin is removed from the treatment process from the settler underflow and generally transferred to one of two large regeneration vessels. When one vessel is filled the settler underflow stream is directed to the second regeneration vessel while the one that has been filled undergoes regeneration.
- the regeneration is performed either in: (i) a mixing tank where a mechanical agitator mixes the regenerant solution s with the resin (agitated tank regeneration), or (ii) a tank where the regenerant solution is passed through a stationary bed of resin with the ion exchange occurring while the regenerant is in contact with the resin
- fixed bed filtering systems retain the resin within large treatment vessels and the resin is regenerated by taking the treatment vessel offline and washing the loaded resin with a suitable regenerant to regenerate the resin.
- Each step in the regeneration process can take a long time to complete.
- Large regeneration tanks may need to be filed with resin and regenerant, then allowed time to regenerate the resin, then the regenerant needs to be drained and the resin washed before recycling the regenerated resin.
- Large qualities of regenerant, typically brine, are used and result in large quantities of spent regenerant containing the compounds such as DOC and other electrolytes that were bound to the ion exchange resin together with electrolytes ordinarily present in the regenerant.
- Large volumes are involved as the regenerant needs to be used in a dilute solution because ion exchange resins suffer from osmotic shock which damages the resin reducing its effectiveness.
- regenerant precursor solutions are normally diluted before use as regenerant and therefore increases the total volume of spent regenerant.
- the washing step also produces a waste stream containing dilute concentrations of electrolytes ordinarily present in the regenerant.
- the spent regenerant and wash waste stream may need to be collected, processed, treated or concentrated and removed by tanker for disposal.
- tanker At many sites it is not environmentally acceptable to send large qualities of brine into the sewers / drain system. This increases the overall capital and maintenance costs due to the additional required equipment for managing the dilution of the regenerant precursor solution, pumps, storage vessels and associated sensors and other equipment.
- the treatment plant requires a large inventory of resin to cover both the resin in use in the water treatment process and also the resin being regenerated and spare resin to replace operating losses.
- This resin will need to be stored on site. This can create further difficulties when the plant is shut down for maintenance. All the resin needs to be stored in containment vessels whilst the water treatment tank is subjected to maintenance.
- the additional systems required for on site regeneration of loaded resin are a significant problem and may prevent the use of resin systems at some water treatment sites.
- the overall regeneration systems can have a large footprint as the amount of loaded resin which can be regenerated at any one time has traditionally been limited by the size of the regeneration containment vessel. Large vessels have a large footprint and the required space may not be available at the treatment plant, limiting the regeneration process to vessels of restricted sizes or requiring the loaded resin to be processed off site.
- the cost associated with manufacturing the large containment vessel(s) often require specialised design, engineering, manufacture and equipment which can also significantly increase the initial installation costs and time particularly when the customer has little expertise with on site resin regeneration.
- the present invention is based around the concept of regenerating smaller qualities of loaded resin using counter current and plug flow systems.
- Such a regeneration system can allow for the regeneration of a larger quantity of resin more quickly and with less waste than a comparative large scale batch system.
- a process for the regeneration of loaded ion-exchange resin such as resin loaded with dissolved organic carbon (“DOC"), the process comprising: (a) providing loaded resin for regeneration;
- step (j) once a third stage regeneration vessel has been filled, contacting the second stage regenerated resin therein with third stage regenerant in a plug flow to provide the regenerated resin; wherein after contacting the resin in step (j), the third stage regenerant is collected and added to the first stage regenerant.
- the above processes may further include additional steps associated with ion-exchange processes for water treatment, as would be understood by a person skilled in the art.
- the regenerated resin in the third stage regeneration vessels may be subjected to a rinsing stage to replace the regenerant with a suitable transfer fluid for subsequent use in a water treatment process.
- a suitable transfer fluid may be raw water.
- Conductivity sensors may be used to detect when sufficient regenerant has been removed. This allows the used third stage regenerant to be removed, collected and recycled as first stage regenerant.
- the loaded resin will be provided together with a transfer fluid, which may be the water being subjected to the ion exchange filtration treatment. It is thus preferable if the process includes the additional step of concentrating the resin ' (increasing the amount of resin in the transfer fluid) before filling a first stage vessel with the loaded resin. Likewise, it can be preferable to concentrate the resin before the resin is used to fill the third stage vessels. This can be a useful step as the concentration of the resin soaking in regenerant in the second stage may vary depending on the concentration of the resin in the first stage vessels.
- the concentration step can be performed by including a concentrator, such as a settling vessel, into which passes resin within a fluid. At least a portion of the resin settles within the vessel and with the excess and the fluid overflowing the vessel.
- concentrators before filling the first and third stage vessels may also permit the regulation of the regeneration process.
- the concentrators could be set to fill the first and third regeneration vessels depending on the availability of empty vessels or based on a desired concentration of resin or a combination of factors. If a vessel is not available then the concentrators will improve the efficiency of the next filled vessel by concentrating the resin whilst awaiting the next available empty vessel. The concentrator will then deliver more concentrated resin into the next empty vessel for subsequent processing.
- the transfer fluid is removed from the first and also third stage vessels (in the latter the transport fluid is first stage regenerant), after they have been filled with resin and before respectively contacting the resin with first and third stage regenerant. Whilst gravity may be used to drain some transfer fluid from the vessels it is preferred to more quickly remove transfer fluid from the vessels by a suitable fluid extraction means, such as a pump. It is not necessary to removal all of the transfer fluid (nor is it considered possible) but the removal of a significant proportion of the transfer fluid so the resin bed is exposed, can improve the overall plug flow performance and avoid the unnecessarily dilution of regenerant.
- the extraction means can continue to operate as the regenerant is applied to the resin, to draw the regenerant through the resin in a plug flow.
- the extraction means is a pump, such as a vacuum pump.
- the outflows from the first and third stage vessels include sensors to monitor the fluid outflows (transport fluid and regenerant).
- Conductivity sensors can be used to detect the change in concentration.
- the use of plug flow results in less mixing of fluids and can provide clear interface between the fluid types which may be detected with conductivity sensors.
- the second stage soaking regeneration step is omitted. Accordingly, in this aspect there is provided a process for the regeneration of loaded ion-exchange resin, the process comprising:
- step (f) once a first stage regeneration vessel has been filled, contacting the loaded resin within the vessel with first stage regenerant in a plug flow to provide a first stage regenerated resin; (g) transferring the first stage regenerated resin from a first stage regeneration vessel into a third stage vessel; (h) contacting the first stage regenerated resin in the third stage vessel with third stage regenerant in a plug flow to provide the regenerated resin; wherein after contacting the resin in step (h), the third stage regenerant is collected and added to the first stage regenerant.
- an intermediate storage vessel for at least collecting the resin from the first stage regeneration vessels before the resin is transferred into the third stage vessels.
- One of the benefits of the present invention is it can be used to provide a substantially continuous regeneration process with continuous inflow of loaded resin and outflow of regenerated resin suitable for use in a water treatment process.
- step (s) repeating step (m) whenever there is an empty third stage vessel and sufficient resin to fill the vessel in the third stage concentrator.
- a continuous outflow of regenerated resin in a suitable transport fluid may be provided from the storage vessel for addition to a water treatment process.
- the process is incorporated within an ion exchange water treatment process and the transport fluid in step (h) is water from the treatment plant.
- the excess transport fluid (water) overflowing the first stage concentrator and from any filled first stage regeneration vessels may be returned to the treatment plant for subsequent treatment with resin (fresh or regenerated).
- the transport fluid portion removed from first stage regeneration vessels may be returned to the treatment plant until regenerant is removed from the first stage regeneration vessels.
- the removal of regenerant may be detected by an appropriate sensor for the regenerant, such as a conductivity sensor for use with brine regenerant.
- the removal of regenerant may also be determined based on outflow or volume and based on historical precedents.
- the process operates in a counter current manner, with new regenerant being added to the process as third stage regenerant.
- the used third stage regenerant containing some removed electrolytes is added to the first stage regenerant.
- DOC removal a proportion of the regenerant removed from the first stage regeneration vessels could be sent to waste to dispose of the extracted DOC. It is preferred to separate the first portion of the regenerant removed from the first stage regeneration vessels from the remainder of the regenerant removed from the first stage regeneration vessels.
- the first portion will contain a high concentration of the compounds which were loaded on the resin and this may be sent to waste or otherwise removed from the regeneration process.
- the remainder of the used first stage regenerant may be re-used as first stage regenerant.
- the first portion containing the highest concentration of the compound loaded on the resin may be separately processed to recover the valuable elements therein.
- the volume of the first stage regenerant removed from the process should be matched to the volume of liquid added to the first stage regenerant from the third stage vessels.
- the resin may be re-fluidised by injecting a suitable transport fluid into the vessel.
- a suitable transport fluid would be regenerant for use in the first stage vessels.
- the excess fluidising regenerant could be flushed through with the resin into the second stage vessel which contains the same regenerant.
- the regenerated resin could be fluidised with rinse transport fluid suitable for use in subsequent ion-exchange processes.
- the transport fluid may be raw water in a DOC removal process.
- the processes could also be conducted by using a multi-function vessel, which operates as both the first stage and third stage vessel.
- the second stage regeneration vessel could be omitted or incorporated into the multi-function vessel.
- a process for the regeneration of loaded ion-exchange resin such as resin loaded with dissolved organic carbon (“DOC"), the process comprising:
- the action of the second stage vessel can be incorporated into the regeneration vessel by simply allowing the resin to remain soaking in first stage regenerant whilst in the regeneration vessel. This may not be desirable as it will further slow down the overall regeneration process, unless the system includes a number of multi-function regeneration vessels.
- a process for the regeneration of loaded ion-exchange resin comprising: (a) providing loaded resin for regeneration in a holding vessel; (b) providing first stage and third stage regenerant suitable for regenerating loaded resin;
- the holding vessel may be a concentrator vessel which increases the concentration of the resin within the transport fluid by allowing excess transport fluid to overflow the concentrator, or may be coupled to a concentrator vessel.
- an arrangement of apparatus for use with above regeneration processes would include appropriately connected vessels, pipes, valves and sensors for operating the above described regeneration processes.
- the apparatus includes a module containing array (three or more) first stage vessels or third stage vessels together with associated operation systems.
- a modular system could allow a number of additional modules to be connected together to improve the regeneration rate of the resin.
- a modular system could allow for standardisation of regeneration systems and enable the use of the same overall process with ion-exchange treatment plants of various resin throughput largely by changing the number modules. This could simplify maintenance and reduce associated costs,
- the method could be operated to use lower concentrations, such as 5% or 10% wt/wt, and could be used with the third stage regenerant at a similar or the lower concentration than the first stage regenerant. In the latter case the method may require the addition of concentrated regenerant to compensate for the loss of concentration from the addition of third stage regenerant and any rinse portion.
- Fig. 1 is a schematic diagram of a regeneration process of the present invention showing apparatus and the movement of resin and regenerant and other fluids.
- Fig. 2 is a schematic diagram of a series of first stage regeneration vessels for use in the process of the present invention.
- Fig. 3 is a schematic diagram of a single first stage regeneration vessel for use in the process of the present invention.
- Fig. 4 is a schematic diagram of a series of third stage regeneration vessels for use in the process of the present invention.
- Fig. 5 is a schematic diagram of a single third stage regeneration vessel for use in the process of the present invention.
- Fig. 6 is a schematic diagram of a salt saturator vessel, for use in conjunction with the process of the present invention.
- Fig. 7 is a schematic diagram of a regeneration vessel, which can be used in the process of the present invention.
- Fig. 8a and 8b are schematic diagrams respectively showing side and end elevations of an arrangement of apparatus for use in the process of the present invention.
- Fig. 9 is a schematic diagram of a regeneration process of the present invention in accordance with example 2.
- Fig. 10 is a graph of conductivity (ms/cm) against the number of bed volumes (BV) of regenerant drained through various resin bed heights. Four sets of results are shown depicting 200mm (diamond), 200mm (square), 300mm (triangle) and 500mm (X) runs.
- Fig. 11 is a graph of conductivity (ms/cm) against the number of bed volumes of rinse water drained through various resin bed heights. Three sets of results are shown depicting 200mm (diamond), 300mm (square) and 500mm (triangle) runs.
- Fig. 12 is a graph of conductivity (ms/cm) against the number of bed volumes (BV) of regenerant leaving the column after 1 st (diamond) and 4 th (square) regeneration.
- Fig. 13 is a graph of conductivity (ms/cm) against the number of bed volumes of rinse water leaving the column after 1 st (diamond) and 4 th (square) regeneration.
- Fig. 14 is a graph of UV absorbance at 254nm (cm "1 ) against bed volumes (BV) of regenerant after 1 st (diamond) and 4 th (square) regeneration.
- Fig. 15 is a graph of UV absorbance at 254nm (cm '1 ) against bed volumes (BV) of rinse water after 1 st (diamond) and 4 th (square) regeneration.
- Figs. 16a and 16b are photographs of samples of end regenerant from the stage one regeneration vessel 210 and the rinse water from the stage three vessel 212.
- Fig. 17 is a schematic diagram of the layout of a transfer vessel, contactor, and regeneration vessel assembly.
- Fig. 18 is a schematic diagram of a splitter box and transfer vessel arrangement.
- Fig. 19 is a schematic diagram depicting a regeneration process of the present invention using multi-function regeneration vessels.
- Fig. 20 is a graph of volume (%) and particle diameter ( ⁇ m) of virgin resin (square, solid line) and virgin resin subjected to treatment cycles with saturated brine (circle, broken line).
- Fig. 21 is a graph of volume (%) and particle diameter ( ⁇ m) after attrition of virgin resin (square, solid line) and virgin resin subjected to treatment cycles with saturated brine (circle, broken line).
- Figs. 22a and 22b are a pair of photographs of samples of virgin resin.
- Figs. 23a and 23b are a pair of photographs of samples of cycled virgin resin.
- regenerating ion-exchange resin or "regenerating resin”, as used herein refers to a process in which the ion-exchange capacity of a loaded (also referred to as spent or used) ion-exchange resin is returned to a level whereby it is rendered suitable for use in subsequent ion-exchange processes.
- the water treatment plant may be a plant for producing potable water for distribution and consumption, or may be a plant for the treatment of sewage or industrial water treatment.
- An industrial water treatment plant may be associated with food processing, pharmaceutical production, electronic component manufacture, membrane plant rejects (usually derived from nanofiltration or reverse osmosis processing), hospital applications, power generation and the like.
- the resins in the water treatment plant may be used to remove undesirable compounds from the water or may be used to concentrate and collect desired compounds.
- ion exchange resins have been used to concentrate valuable elements (such as gold, silver and uranium). While the present invention is useful in any large scale water treatment facility, it is particularly preferred for use in the treatment of a water source to produce potable water for distribution and consumption.
- the preferred ion-exchange resin, MIEX DOC ® Resin, is used in the removal of DOC and has cationic groups which provide suitable sites for the adsorption of the DOC. These cationic groups have associated anions which exchange with the DOC during the ion- exchange process.
- the regeneration process of such ion-exchange resins typically involves the displacement (or exchange) of the adsorbed DOC with chloride ions provided by a regenerant.
- Ion-exchange resins used in the removal of other types of compounds from water may have other types of groups and require different types of regenerants. For example Dowex ion exchange resins may be used to separate uranium from liquid media for mining and water remediation purposes.
- the ion exchange resins are normally used in fixed bed and continuous counter current systems. These type 1 resins (strong base anion resins) can be used to remove uranyl ions from water and can be regenerated with chloride ions, acidified nitrate solutions and sulphuric acid solutions. Similar types of resin systems may be used to remove hexavalent chromium from ground water (such as Purolite A-600) which can be regenerated with brine.
- DOC loaded ion-exchange resin may be regenerated by contact with a suitable regenerant, such as an aqueous chloride salt solution which allows the chloride ions to exchange with the DOC adsorbed on the resin.
- a suitable regenerant such as an aqueous chloride salt solution which allows the chloride ions to exchange with the DOC adsorbed on the resin.
- the preferred chloride salt is NaCl although other chloride salts can work.
- the most preferred regenerant for use with MIEX ® is brine (substantially a NaCl solution).
- the regeneration of DOC loaded MIEX DOC ® resin is carried out with an aqueous chloride salt solution in which the initial chloride salt concentration (as used at the third stage of regeneration) is more than 1.5M, or more preferably 2M or greater.
- the process of the invention can provide for continuous or near continuous inflows and outflows of loaded and regenerated resin respectively, although the process incorporates batch processing steps within an overall processing system.
- a continuous stream of resin can be fed into an initial vessel from which the loaded resin is subjected to batch regeneration processes within the regeneration system and delivered into a storage vessel from which a continuous flow of regenerated resin can be returned to the treatment plant.
- the present invention includes a multi-stage regeneration system which comprises a first regeneration stage, an optional second soaking regeneration stage and a third regeneration stage.
- the third regeneration stage may be followed by rinsing / washing step.
- the difference between the first and third regeneration stages is related to the concentration of the regenerant solution which passes from the third stage to the first stage (and may also be used as the soak regenerant in the second stage).
- the regenerant used in the third stage may be of a stronger regenerant concentration than that used in the first stage and this is achieved in practice by directing the flow of regenerant, after coming into contact with resin in the third regeneration stage, to the first stage. This provides a counter current flow and in addition to improving the effectiveness of the regeneration process, it may also provide another benefit in that the treated resin does not initially come into contact with highly concentrated regenerant which may cause osmotic shock and damage the resin.
- the first and third regeneration stages are preferably conducted in separate regeneration vessels, although it is envisaged that the process could be conducted within the same vessel, although this would increase,, the complexity of the plumbing.
- the use of specialised first and third vessels should provide process efficiencies, particularly with larger qualities of resin. It also offers the advantage of the intermediate soaking phase in the second vessel.
- the use of multi-function regeneration vessels can offer benefits in plant cost and footprint, and offers advantaging in flow control despite the need for additional control plumbing.
- the second stage soak tank can be effectively provided by allowing the resin to sit in first stage regenerant after drawing off the initial portion of the regenerant.
- the soaking step would slow down the processing of the resin, it can be an option when the regeneration system has unused capacity, which can happen when the water treatment plant is running at reduced rates or because the regeneration plant has available multi-function vessels at the relevant time.
- the process would include a soaking step of variable length, with the length being governed by the overall regeneration process rates, and the needs of the water treatment plant.
- multiple regeneration vessels in order to permit the simultaneous processing of loaded resin through the regeneration process.
- resin in a first stage vessel can be contacted with regenerant, whilst resin may be added to another first stage vessel and whilst excess raw water may be removed from a further first stage vessel.
- multiple third stage regeneration vessels may be used to improve the processing rate of the regeneration step and any washing / rinsing step.
- the resin in a third stage vessel may be contacted with the regenerant, the regenerated resin in another vessel may be subjected to a rinsing step whilst yet another third stage vessel is filled with resin.
- first and third stage vessels required for efficient operation will depend on a number of factors such as the type of resin to be regenerated, the amount and nature of the chemicals to be removed from the water, the throughput of the treatment plant, the effectiveness and pumping rate of the pumps used to extract water and regenerant and the size (capacity) of the regeneration vessels.
- first and third stage vessels are separate and distinct vessels.
- the invention also includes the use of multi-function regeneration vessels, where the multi-function vessel can function as either a first or third stage regeneration vessel.
- the same advantages can also apply when using multiple multi ⁇ function regeneration vessels.
- first or third stage vessel includes the use of a multi-function vessel respectively operating as a first or third stage vessel.
- Reference to a second stage vessel includes the use of a separate second stage vessel as earlier described in conjunction with the multi-function vessels, but also includes the use of a multi-function vessel as a limited second stage vessel by simply allowing the resin to soak in the regenerant.
- the vessels may take the form of columns, tanks (including mixing and/or settling tanks) and the like.
- the regeneration vessels will be standardised in size, and the use of two standard sizes is envisaged - 600mm (2ft) by 600mm by 1800mm tall (6ft) and 1200mm (4ft) by 1200mm by 1800mm.
- the tanks are square or round with a resin bed height set at 600mm (2ft).
- the regeneration vessels take the form of mixing tanks may be fitted with a mechanical stirring device.
- each regeneration vessel may be fitted with separate inlet valves to allow for the addition of resin, regenerant, and optionally water, into the regenerant . vessel.
- one or more of the resin, regenerant and water may be fed into the vessels via a common inlet valve connected to a feed pipe connected to separate resin, regenerant and water feeds.
- Each feed pipe may have separate closures or a downward arrangement of feed pipes together with gravity can be used prevent the feeds intermixing and backflow.
- the inlet valves are positioned at the top of the vessels.
- At the base of each regeneration vessel is an outlet valve, which allows for the removal of the aforementioned elements from the regeneration vessel.
- Regeneration is effected by filling a regeneration vessel with resin and transfer fluid (typically untreated water for the first stage or recycled regenerant for the third stage) via the resin or common inlet valve.
- transfer fluid typically untreated water for the first stage or recycled regenerant for the third stage
- excess transfer fluid is removed by a suitable means such as by vacuum pump and a predetermined quantity of regenerant (which may be determined by mass, flow rate or volume) is then added to the resin.
- the regenerant may be allowed to contact the resin for a time before being moved through the vessel as in plugflow.
- the regenerant is simply added and moved through resin in a plugflow as soon as the excess transfer fluid has been removed.
- the vacuum pump could remain in operation as the regenerant is added to the vessel to pull the transfer fluid and then most of the plug of added regenerant.
- a rinse / wash step can be conducted in a similar manner in the third stage vessel.
- the first stage regeneration will normally involve larger volume of regenerant than the third stage regeneration. Available process time is the primary constraint as moving large qualities of first stage regenerant through the first stage vessel would slow down the overall process time and may not significantly improve the regeneration of the resin.
- the first fraction of the first stage regenerant is typically removed from the process and this loss is made up by the addition of regenerant collected after the third stage regeneration step.
- the third stage regeneration of the resin does not require a large volume of regenerant.
- the third regenerant is more concentrated than the first stage regenerant, and may be a saturated solution.
- a low volume of third stage regenerant followed by a rinse solution can be moved in a plug flow through the resin. The use of concentrated regenerant in a plug flow reduces the intermixing of the regenerant into the rinse solution.
- BV bed volumes
- the collected regenerant, diluted by the rinse, (0.2 BV) would then be added to the first stage regenerant.
- the first stage regeneration may involve the application of 1 BV of first stage regenerant and would allow for a first fraction of 0.2 BV to be removed and sent to waste or processing.
- a vacuum pump may be used to pull transfer fluid and a plug of regenerant through the resin, it is envisaged that other systems may also be effective. Where time permits gravity could be used to move the fluids through the vessel. Alternatively a positive pressure could be applied within the vessel to push the fluid and regenerant through the resin. Sensors may be used monitor and regulate the levels of regenerant, resin or water added to the regeneration vessel to avoid overfilling the vessel. Sensors may also be used to monitor the fluid outflows from the vessel. The sensors can be fitted to the inlet and outlet valves and as such can regulate the flows of the aforementioned elements within the regenerant vessels.
- sensors such as conductivity sensors, or measuring outflow volumes and comparison to precedent values (essentially a computerised memory based on look up tables from calibration testing) may allow for highly effectively separation of the types of outflows from the regeneration vessels.
- a conductivity sensor could detect when the plug of regenerant brine has reached the sensor and effect a redirection of the outflow.
- the outflow can be returned to the raw water supply (when the transfer fluid is raw water) or to a supply of first / second stage regenerant (when the transfer fluid is first / second stage regenerant as used with the resin in the third stage regeneration vessels).
- the outflow is the regenerant plug as indicated by an increase of conductivity by the change from raw water to first stage regenerant or from first / second stage regenerant to the more concentrated (and thus more conductive) third stage regenerant then the outflow may be redirected as appropriate.
- the outflow of the third stage vessel could again be redirected when the plug of rinse water passes through the vessel.
- the sudden drop in conductivity would signal a need to redirect the output or to simply empty the third stage vessel of washed and regenerated resin.
- the use of sensors in this manner combined with a switching system to redirect outflows may provide substantial improvements in the regeneration process as it avoids discarding unnecessary fractions and avoids unnecessary dilution of the regenerant.
- the first fraction of regenerant from the first regeneration vessels will contain the most concentrated mixture of the chemical which was loaded on the resin in used regenerant. Depending on the process, this fraction could be sent to waste disposal (for DOC) or retained for subsequent processing (to recover useful chemicals). The remainder could be returned to a first / second regenerant storage vessel for subsequent re-use.
- the regenerant from the third stage vessel can all be sent to a storage vessel for use as first / second stage regenerant, although it is possible that the portion of the latter more concentrated third stage regenerant could be recycled as third stage regenerant.
- the latter option may be complex as it may require adding the initial fraction (containing highest concentration of exchanged electrolytes) to the first stage regenerant, recycling the bulk fraction and then adding the end fraction covering the interface between the third stage regenerant and a rinse solution.
- the regenerant is brine
- the start of the end fraction could be sensed by a decrease in conductivity due the dilution of the brine with a water rinse solution.
- the outflow could be redirected so to send any excess rinse solution back into the raw water supply (or simply trigger the emptying of the third vessel).
- the overall regeneration process could thus be controlled by a programmable machine.
- One of the benefits of having multiple vessels is that it is possible to service selected vessels without shutting down the whole regeneration system (and possibly the treatment plant). Individual vessels could be taken out of service for maintenance and, depending on the size of the regeneration system, the other components of the system could compensate.
- the loaded resin is initially fed from the contactors (or settlers associated with the contactors as described in WO 96/07615) of a water treatment plant into a concentrator.
- the concentrator is transfer vessel with a conical shaped base. Any excess water may overflow the rim or through apertures in the walls and can return back to the raw water contactors. This can be achieved via the use of a pump or by simply locating the concentrator above the contactors in the treatment plant. It is preferred to locate the concentrator transfer vessel at a position higher than the first stage regeneration vessels so the concentrated loaded resin may be gravity fed into these vessels.
- the concentrator can also take the form of a resin transfer tank, which would accumulate and thicken loaded resin removed from a contactor collected at the settler.
- the transfer tank could receive side-stream or a timed split, or the entire flow from the resin recycle pump (or at least one pump in multiple pump systems).
- the return flow of resin from the settler could pass through a splitter box which directs a portion, in the order of 5 to 15% into the transfer tank, with the remainder being returned to the contactors.
- the splitter box is an open channel with an adjustable gate to diver a set portion of the return resin flow into the transfer tank. It would be possible to divert all the resin into the transfer tank but it may be more practicable to divert only some of the resin.
- the transfer tank would be located such that its top water level is above the contactor(s) water level and allow excess resin and water to overflow to the contactors.
- There will be two sources of overflow from the transfer tank to the contactors - one from the transfer tank itself as in a typical overflow arrangement and the other from the splitter box used to divert a portion of the resin to the transfer tank with the majority of the return flow proceeding to the contactors.
- This concentrator system avoids the need for a flow meter and controls to divert the required resin volume to regeneration from the settler.
- the transfer tank can continuously accumulate and thicken resin, with the excess of resin overflowing back into the contactors, as the regeneration rate will be determined by the availability of regeneration vessels.
- the resin transfer tank may concentrate the resin to about 500-700ml/l before sending it to the regeneration tanks.
- the resin in another concentrator transfer vessel before subjecting the resin to third regeneration stage. This may be useful if the resin has been physically moved from a first stage regeneration vessel. The excess regenerant can simply overflow the concentrator (the rim or via apertures in the side wall) and would gravity feed back into the first stage regenerant storage tank. It would be preferred to have the third stage concentrator vessel located above the third stage regeneration vessels to permit the gravity filling of the third stage vessels with the resin.
- a second resin regeneration stage in the form of a resin storage tank between the first and third regeneration stages.
- the storage tank is preferably fitted with a mechanical stirrer to effect efficient mixing of the regenerant and resin.
- the regenerant which fills this resin storage tank may result from the first stage regenerant storage tank, and particularly any overflows from that tank, and the regenerant overflow from the third stage concentrator.
- An advantage of adding the storage tank is the additional soak or contact time in the regenerant allows for more effective regeneration.
- such a storage tank would provide a convenient location for the operator to store the inventory of resin in brine regenerant if the entire system is shut down for maintenance. Storing the resin in a regenerant (brine) solution can avoid the problems associated with the build up of microbial deposits which can occur if the resin was stored in fresh water.
- the regenerated resin may be directly returned to the contactors, or may be stored in a fresh resin storage tank, which may be conveniently located above the contactors. Fresh resin can then be gravity discharged from the storage tank into the contactors and, in the event of a system failure, resin overflowing from the storage tank will also feed into the contactors.
- the regeneration system could be used to regenerate fixed bed resin systems, continuous counter current resin systems as well as a fluidised resin system made possible with MIEX ® resin.
- the regeneration system may be used alone or in conjunction with membrane filtration techniques.
- the regeneration system may be incorporated into the overall process of existing ion- exchange treatment plants. It may be used in conjunction with ion exchange resin processes combined with membrane filtration systems. The combined treatment and regeneration process with ion exchange resin may improve the effectiveness of the membranes, increase the flux across membranes and reduce operating costs. For new installations it may be used where existing membrane filtration techniques are replaced with ion-exchange techniques.
- the present invention can be used where ion-exchange processes are incorporated to significantly reduce the size and hence capital and operating cost of a membrane filtration plant.
- the reduction in capital and operating costs may enable consideration to be given to the installation of membrane filtration rather than coagulation/ sedimentation plants thereby substantially reducing the size of the plant and enabling the production of potable water without the addition of chemicals other than for disinfection purposes.
- Examples of water treatment processes involving ion-exchange are disclosed in WO96/07615, and the present regeneration process can be readily incorporated into these processes.
- the invention also provides an industrial scale process for the removal of DOC from water containing DOC, said process comprising:
- the present invention provides an industrial scale process for the removal of DOC from water containing DOC, said process comprising:
- step (iv) returning the regenerated resin back to step (i).
- the raw water is generally fed into a continuously stirred tank (the contactor) which has a nominal residence time usually of between about 5 and 60 minutes.
- the magnetic ion-exchange resin is added either directly into this tank or into the raw water in the pipeline feeding this tank. It is in this tank that the majority of the ion-exchange process occurs.
- the water Prior to treatment with the ion-exchange resin the water will generally have been screened to remove large particles to protect pumps involved in pumping the water to the treatment plant. It is also possible that the water will have been subjected to one or more pretreatment steps, such as coagulation / flocculation and subsequent clarification.
- the resin and water (resin suspension) is generally passed to a separating stage (settler) where the resin can be recovered and regenerated and/or returned.
- a separating stage such as a mixer
- the resin can be recovered and regenerated and/or returned.
- gravity sedimentation Depending on the density of the resin it may be possible to recover it using gravity sedimentation.
- magnetic ion-exchange resins have a strong tendency to agglomerate to form large and fast settling particles, when shear is removed (as occurs in the settler). The agglomerated resin particles settle rapidly and are collected on the bottom of the settler where they may be transferred (eg. by pumping) back to the head of the treatment plant for reuse in the process.
- At least some (and generally a small portion) of the flow which is returned back to the head of the plant can be subjected to the regeneration process of the present invention.
- fresh, regenerated resin is added to the contactor to make up for the resin not being returned.
- the present invention allows for this process to be done in a continuous manner. This ensures the performance of the process is maintained.
- ion-exchange resin After separation of the ion-exchange resin from the water it is usual to subject the water to further processing before it is suitable for distribution and consumption.
- the water may be subjected to a coagulation / flocculation step followed by clarification.
- coagulants such as alum (aluminium sulphate), iron salts and synthetic polymers are used following the ion-exchange step.
- the water may also be subjected to one or more of the filtration steps described above, as well as disinfection.
- the disinfectant may be added at any stage during the water treatment process. Usually however, disinfectants are added during or at the end of the treatment process such that there is residual disinfectant present in the water supplied to the consumer. This is known as secondary disinfection and most commonly involves the use of chlorine, chloramines and chlorine dioxide.
- potassium permanganate, peroxone, UV radiation and combinations of the above can also be used as primary disinfectants.
- the water treatment process may also be used in conjunction with other unit processes such as ozonisation and treatment using granular activated carbon (GAC).
- GAC granular activated carbon
- the regeneration processes of the present invention may be utilised in the above described treatment processes or similar treatment processes, involving an ion-exchange process.
- inorganic compounds and organometallic compounds can be removed by using appropriate ion exchange resins, such as described in US Patent Application 11/124,624 entitled “Inorganic Contaminant Removal from Water", filed on6 May 2005 by Bourke and Nguyen and incorporated by cross-reference, and these ions include perchlorate, sulfate, nitrate, phosphate, phosphite, bromide, bromate, arsenic, chromium and barium ions. These waters can then be used in a wide range of applications such as boiler feedwater, potable water or as high quality process water for the pharmaceutical manufacture, electronic component manufacture and the chemical industry. The regeneration process may be useful in these applications.
- the resin regeneration system depicted in Fig. 1 consists of two settler tanks (Sl and S2) which have conical shaped bases, first stage of regeneration vessels (RV) fitted with mechanical agitator/mixer (MV), second stage regeneration vessel (RU), fitted with an agitator / mixer (MU), and third stage regeneration vessels (RT), fitted with an agitator / mixer (MT).
- the system also comprises regenerant storage tanks (RSl and RS2), a salt saturator (SS), and a series of pumps (PV, PU, PT, PF and 160).
- RV and RT each comprise an array of vessels as shown in Fig 2 and 4.
- RU is a single vessel.
- the resin settles in Sl with the raw water overflowing back to the raw water treatment plant contactors via the overflow line (3).
- the Sl tank can also operate as a concentrator whereby the concentration of resin in the tank is increased.
- Sl is also fitted with an outlet valve (5) at its base, which is connected to a common manifold (46) to supply RV.
- RV When RV is ready it will open its resin inlet valve (BI) and fill with resin/water from Sl. Since Sl fills to a set level, RV cannot be overfilled with loaded resin.
- the loaded resin will usually contain amounts of water left over from the water treatment process. Accordingly, once filled RV is de-watered using its associated vacuum pump (PV). This raw water can be directed back to the contactors via line (68). Once the loaded resin bed is exposed, regenerant is added to RV from RSl at constant pressure by opening an inlet valve (BI) for a set period. The regenerant from RSl is supplied by pumping (PT) the used regenerant from RT via common regenerant discharge line (134).
- PV vacuum pump
- Water is removed from the resin bed of RV is directed to the contactors via line (68) until salt is detected (using a conductivity sensor) at which time the fluid is diverted to the waste treatment/disposal system via waste treatment / discharge line (70).
- the regenerant could be used in more than one regeneration cycle. In such arrangements the initial portion of the regenerant (containing the highest concentration of BOC) may be to waste with the reminder recycled to RS 1.
- regenerant which is sourced from the overflow of RSl via the regenerant storage tank overflow line (10) and the settler tank S2 via the settler tank overflow line (11).
- the resin/regenerant is pumped (PU) via line (6) into S2.
- the resin is allowed to settle (thicken) before being transferred to RT.
- S2 is also fitted with an outlet valve (12) at its base, which is connected to a common line (108), which is connected to the resin inlet valve (IR) of RT.
- RT When RT is ready it will open its resin inlet valve (IR) and fill with the resin in S2. Since S2 also fills to a set level, RT cannot be overfilled with resin.
- the fresh regenerant inlet valve (RE) is opened and RT is filled with fresh regenerant via a constant pressure line (106).
- the regenerant is then pumped (PT) from the resin bed and directed via (134) to RSl, while water inlet valve (IW) is open. This adds water from a common water line (110) to the resin bed to wash the remainder of the regenerant from the bed.
- Fresh regenerant is prepared in (RS2) by transferring by pump (160) a saturated salt solution, for example brine, from SS via saturated feed line (162) to RS2, and then diluting to a desired concentration through the addition of water from water feed line 17. Salt and water are added to the saturator SS by feed lines 152 and 154 respectively,
- Fig. 2 depicts a series of first stage regeneration vessels (RVl-R V6).
- Each of the vessels is connected to a resin delivery line (46) and a regenerant supply line (44).
- Each of the vessels is also fitted with inlet valves for both the resin (RI1-RI6) and regenerant (BIl- BI6), and a mechanical impeller agitator and motor (MV1-MV6).
- the vessels are also fitted with a discharge pipe (D1-D6), which directs resin through a resin outlet valves (RM1-RM6) to a common resin outlet line (26).
- V1-PV6 valve directed air pumps
- the fluid discharge can be directed to a common raw water contactor line (68) or waste treatment/discharge line (70).
- Each pump is also fitted with a common air supply line (60).
- the dashed lines signify that the vessels can be set up in a transportable module like a shipping container and if required, two such transportable modules can be placed side by side and connected in order to increase the regeneration capacity of the system.
- Fig. 3 depicts a single first stage regeneration vessel (RV) fitted with two TEE connectors (40) and (42) respectively fitted to regenerant supply line (44) and resin supply line (46). The lower ends of TEE connectors are located within the regeneration vessel.
- the supply lines are isolated by valves (48) and (50), which are used to regulate the flow of regenerant and resin respectively. These valves can be ball valves, for instance George Fisher Actuated valves.
- the regeneration vessel can be any suitable commercially available vessel, for instance an E66 Nylex tank.
- the regeneration vessel itself is of uniform dimensions and is fitted with a mechanical stirrer (52) and a drainage screen (not shown).
- a discharge line (54) which is connected to an air pump (56) via valve (66).
- the air pump is connected via an air supply isolation valve (62) to an air supply pipe (60) fitted with an air supply solenoid (58).
- the valve (66) regulates removal of fluids from the vessel.
- the fluids removed through valve (66) can be returned to raw water treatment contactors via line (68) or sent to waste via line (70).
- the lines are regulated by the insertion of appropriately placed valves (72) and (74).
- a separate resin discharge line (64) is connected to the base of the vessel above the drainage screen.
- the line is fitted with a valve (65), which can be a ball valve, and is used to remove the resin from the vessel.
- the resin passes into the common resin discharge line (26).
- Fig. 4 depicts a series of third stage regeneration vessels (RT1-RT6).
- Each of the vessels is connected to a resin delivery line (108), regenerant supply line (106) and water line (110).
- Each of the vessels is also fitted with inlet valves for the resin (IR1-IR6), regenerant (RE1-RE6) and water (IW1-IW6), a mechanical impeller agitator and motor (MT1-MT6) and a drainage screen.
- Each vessel is also fitted with a discharge line (DMl- DM6), which directs resin through a resin manifold (AM1-AM6) to a common resin outlet line (86).
- PT1-PT6 valve directed air pumps
- the fluid discharge can be directed to a common regenerant discharge line (134).
- Each pump is fitted with a common air supply line (126).
- the dashed line signifies that the vessels can be set up in a transportable module like a shipping container and if required, two such transportable modules can be placed side by side and connected in order to increase the regeneration capacity of the system.
- Fig. 5 depicts a single third stage regeneration vessel (RT) fitted with three TEE connectors (100), (102) and (104) respectively fitted to regenerant supply line (106), resin supply line (108) and water supply line (110).
- the lower ends of TEE connectors are located within the regeneration vessel.
- the supply lines are isolated by valves (112), (114) and (116), which are used to regulate the flow of regenerant, resin and water respectively.
- These valves can be ball valves, for instance George Fisher Actuate valves.
- the regeneration vessel (RT) can be any suitable commercially available vessel, for instance an E66 Nylex tank.
- the regeneration vessel itself is of uniform dimensions and is fitted with a mechanical stirrer (118) and a drainage screen (not shown).
- a discharge line (120) which is connected to an air pump (122) via valve (132).
- the air pump is connected via an air supply isolation valve (128) to an air supply pipe (126) fitted with an air supply solenoid (124).
- the valve (132) regulates removal of fluids from the vessel.
- the fluids removed through valve (132) can be returned to the first stage regeneration system via line (134). This line is regulated by valve (136).
- a separate discharge line (129) is connected to the base of the vessel above the drainage screen.
- the line is fitted with a valve (130) and is used to control the removal of resin from the vessel. Suitable valves include ball valves.
- the resin passes into a common resin discharge line (86) for return to the contactor
- control system that could be used with the regeneration system depicted in Fig. 1, 2, 3, 4 and 5.
- Inputs to the control system could include the positions of actuated valves, the readings obtained from conductivity analysers and level sensor readings.
- Each regeneration vessel could be equipped with level sensors and transmitters to provide a continuous reading of tank level.
- the drain pump discharge for each vessel may have a conductivity analyser fitted to the discharge to provide the signal to divert flow when a change from low conductivity to high conductivity is detected.
- a stage one (RV1-RV6) tank is empty in "regeneration completed” status and no other RVl-R V6 tank is filling with resin (if not then wait until a tank is ready)
- Step 1 Open associated resin fill valve (50) Keep valve open until tank high level set point is reached Close resin fill valve
- Step 2 Start drain pump (56) and open associated discharge valve (74) with the water pumped to raw water contactors (68).
- Step 3 Continue drain pump (56) operation until the high conductivity set point is triggerecl - open discharge valve to waste (72) and close discharge valve to contactors (74) and continue drain pump operation until the tank level drops by a set value (stop level equals initial level minus drop value)
- Step 4 Stop drain pump (56) and close associated discharge valve (74)
- a high level alarm in the second stage tank will inhibit all stage one tanks from transferring resin.
- a high level in the second stage tank will automatically reduce the fill set point for regenerant.
- stage three The control methods for stage three are similar to stage one with initial conditions required to be satisfied prior to the initiation of the sequence for each tank.
- the general steps are:
- Step 1 Open resin fill valve (114)
- Step 2 Begin drain pump (122) operation and open discharge valve (136)
- Step 3 Upon a stable level reading, which indicates that the resin bed has been exposed for the second time open water supply valve (116) and fill to set level.
- Step 4 Continue drain pump (122) operation until conductivity of discharge drops below a set value. Stop drain pump (122) and close discharge valve (136).
- Step 5 Start mixer (118) and mix for 5 minutes Open resin discharge valve (130) for set time or until tank level is Om and operate resin pump (PF) and discharge to contactors via line (86). Signal to computer that the "regeneration completed”.
- the second stage tank will be equipped with level and conductivity sensors to provide continuous feedback on the system performance.
- the second stage tank can be monitored for other parameters in the on site lab using established and common process monitoring methods.
- Fig. 6 depicts a salt saturator vessel (150), which is fitted with a salt inlet line (152) and water line (154).
- the water inlet line is fitted with a valve (156).
- a discharge line is fitted to the base of the vessel (158) and the saturated salt solution is pumped via (160) to the second regeneration stage through regenerant line (162).
- the saturated salt solution is prepared by delivering a quantity of salt via (152) to the vessel to form a salt bed at the base of the vessel. Water is added via (154) to maintain a desired level (164).
- Fig. 7 depicts a regeneration vessel (170) fitted with a mechanical stirrer (171).
- the vessel is filled with resin from the stage one regeneration step via a supply line (172).
- Regenerant which overflows from stage one regeneration is supplied to (170) via line (174).
- the level of regenerant/resin in the tank is electronically monitored and regulated with sensor (176) together with the regenerant concentration via an appropriately positioned conductivity meter (178).
- the resin/regenerant is discharged from the base of the vessel and pumped via (180) to second stage regeneration via supply line (182).
- Fig. 8a and 8b depicts a preferred orientation (side and end elevations) of the equipment which comprises a preferred regenerant system of the present invention.
- the system comprises twelve regeneration vessels, six for the first stage (192) and six for the third stage (194), (as shown only the end third stage vessel is visible in the end elevation).
- the combined length of these vessels when connected does not generally exceed 40ft.
- These vessels are positioned on a platform (196) above a fresh resin storage facility (198) and a soak/regeneration vessel (200).
- Above (192) and (194) is positioned resin transfer tanks for the first regeneration stage (202) and the third regeneration stage (204).
- the total combined height of this three level orientation is preferably no more than 25ft (7650mm).
- the system is also fitted with a salt saturator (190).
- Fig. 9 depicts the regeneration process system which is referred to in example 2.
- the system comprises two tall, cylindrical regeneration columns (210), (212) and one agitating mixing tank (214), the agitator is shown as (215).
- the resin is supplied to (210) via (216) and exits the system via (218).
- the regenerant from (214) is transferred via (220) to (210), while the regenerant from (212) is transferred via (222) to (214). Resin is moved from column (210) into tank (214) via (224) and into column (212) via (226).
- a modular package incorporating the equipment necessary to self-install a regeneration system according to the present invention includes components for the set up of the first and third regeneration stages (regeneration modules) and an optional soaking storage tank (soaking module).
- the components which make up each of the first and third regeneration stage modules include six regeneration vessels. Suitable vessels include for instance those supplied by Nylex having a volume of 2.25m 2 , length of 1800mm and height of 1900mm. Other components include 6 regeneration mixers. Suitable mixers are low shear impeller mixers such as those supplied under model type Mixtec HA715 or Lightnin A310. Additional components for the first and second regeneration stages include 2 conductivity meters, for example those supplied under the model type Yokogawa Electrodeless-toroidal (0 to 200mS/cm), one pressure regulator, 20 George Fisher actuated valves, 20 George Fisher manual valves, 6 Solenoid valves (preferably 25mm), and 6 regeneration pumps, (preferably air operated diaphragm valves).
- the optional soaking storage tank module may comprise 1 regeneration tank.
- a suitable vessel may include, for instance, a tank supplied by Nylex having a volume of 17m 2 , length of 2750mm and height of 3500mm.
- the module may also contain a mixer and a resin pump, for instance a LSH pump supplied by Pump Technology.
- This module may also contain a conductivity meter, for example those supplied under the model type Yokogawa Electrodeless-toroidal (0 to 200mS/cm), as well as level meter (Vega - Radar).
- Suitable vessels are those supplied by Nylex (square section) preferably with a volume of 2.25m 2 , length of 1500mm, height of 2000mm and width of 1500mm.
- the modular package may also come with 2 brine storage tanks. Suitable tanks are those supplied by Nylex (circular) preferably with a volume of 2.25m 2 , diameter of 1460mm and height of 1900mm.
- a fresh brine tank may also be supplied. Suitable tanks are those supplied by Nylex (circular) having a volume of 2.25m 2 , diameter of 1460mm and height of 1900mm.
- Other components may include a conductivity meter for the fresh brine tank (Yokogawa Electrodeless-toroidal (0 to 200mS/cm)). Also included may be a levelling meter for the fresh brine tank.
- the modular package may also comprise a salt saturator, pumps for the first stage regenerant, fresh regenerant supply, and fresh resin pump.
- pumps for the first stage regenerant are preferably constant pressure pumps derived from Onga/Grundfos.
- Resin was regenerated using two tall, cylindrical regeneration columns (210) and (212) and one agitated mixing tank (214) as shown in Figure 9.
- the regeneration process is - 43 -
- the resin to be regenerated is allowed to build up in column 210 over a four-hour period, aiming for 2100ml of settled resin each four-hour period. This is just above the 300mm level in the column.
- Initially tank 214 contained 4L of resin with 12L of fresh brine at a salt concentration of 170g/L. From here 1-2BV of brine was transferred to column 210. This was pulled through the column at a flowrate of 116ml/min to obtain a plug flow with a superficial velocity of lm/hr through the resin bed. The first 0.8BV was returned to the contactors. The next 0.4BV was sent to waste. This is the only waste stream from the regeneration process.
- IBV of resin was removed from tank 214 by mixing into a homogenous solution and pumping into column 212. At the same time the drain is left open and the brine is drained into a bucket before being returned to tank 214. Pulling the brine through the bed effectively acts as an extra regeneration step. Resin from column 210 is then transferred to tank 214 with the remaining brine by opening drain point and allowing the resin to slide out. 0.3BV of fresh brine with a salt concentration of
- the table below presents a summary of the plant performance results obtained from a previous trial incorporating the conventional regeneration process and compares it with the results obtained during this trial which utilised the G2 regeneration process.
- Figures 17 and 18 depict the layout of a transfer vessel and splitter box system and the attachment arrangement with a contactor.
- the layout is an example of how the transfer vessel and splitter box system could be installed. This arrangement permits the use of standardised equipment with a wide range of contactors.
- the transfer tank 300 is attached to the side of the contactor 302 and is located above the regeneration system(s) 304 so that resin can gravity feed into the tanks of the regeneration system. Collected resin, such as recycled resin from settling tanks 305, passes along pipe 306 in the direction of the arrow. The resin passes into a splitter box 308, located on the top of the transfer tank 300. The splitter box 308 diverts a desired percentage of the flow, typically 10%, by the use of a gate (not shown) within the box and allows the remainder (90%) to pass via pipe 310 into the contactor 302 completing the return cycle to the contactor of that resin. The flow of diverted resin passes through pipe 312 into the transfer tank 300.
- the tank 300 concentrates the resin by allowing the excess water to pass over the side of the tank into the contactor 302 (overflow shown by line 313).
- the resin concentrates within the tank and settles towards the bottom portion 314 of the tank, which is shaped to direct the resin into a transfer pipe 316.
- the resin flows along the pipe into a regeneration vessel of the regeneration system 304. Once regenerated the resin passes along pipe 318 into a resin storage tank (not shown) for return to the contactor 302.
- the resin storage tank is normally located above the contactor so that the resin can be gravity - 46 -
- the fresh resin is discharged from the fresh resin storage tank 320 into the contactors 302 via discharge pipe 322.
- the rate of discharge from the fresh resin storage tank can be controlled using a manual valve or a timed automatic valve to limit fast discharges of fresh resin to the contactors.
- FIG. 19 depicts an alternative regeneration system incorporating the above improvements and other modifications, discussed in more detail below.
- the regeneration process of the alternative design is carried out in a multi-function regeneration vessel.
- the vessel is connected to a manifold system for use with other multi-function regeneration vessels.
- the alternative system includes the following equipment.
- the exhausted resin may be sourced from the contactor return feed from settlers. However, if a settler system is not required, such as in a column system, then the exhausted resin could be provided by a dedicated exhausted resin feed system.
- Fresh resin tank 320 As described earlier, this is a simple hopper tank which provides a buffer for fresh resin transfer from the regeneration tanks 324, 326 to the contactors 302.
- the fresh resin hopper is located above the contactors connected to the wall of the contactors. In some instances, the fresh resin tank can be eliminated and the regeneration tanks discharge directly into the contactors 302.
- Each tank is equipped with a separate vacuum drain pump 330, 332 and other equipment to enable the tank to be installed on a manifold system.
- the tanks have a standardised design and are available in two sizes depending on plant capacity. The two sizes are 600mm (2ft) and 1200mm (4ft).
- the tanks are square with a resin bed height set at 600mm (2ft).
- the design of the tanks and other equipment is standardised so that a number of identical tanks can be assembled on a common manifold system and additional tanks added as required (eg tank 334).
- the number and size of the regeneration tanks required depends on the resin volume to be processed.
- the table below sets out the estimated number of regeneration tanks for a plant capacity (MGD).
- R600 dimensions are 600mm by 600mm by 1800mm tall - 49 -
- the fresh brine tank receives saturated brine and water in set volumes to obtain a required NaCl concentration.
- the volume of fresh regenerant required for each regeneration is small, and can be about 0.3 bed volumes. Accordingly, the fresh brine tank may be a small tank sufficient to contain 0.3 bed volumes together with volume to fill the delivery pipe at all times.
- the volume of the regenerant discharged from the tank brine can be controlled by a flow level instrument.
- the regenerant system also includes a large regenerant tank 360 for storing the first stage regenerant.
- the fresh brine tank can be located inside the regenerant tank or be attached to the side wall of the regenerant tank.
- the fresh brine tank can be made of welded plastic sheets or be a ready made tank. It is advantageous to locate the fresh brine tank within the regenerant tank as brine would be contained within the regenerant tank in the event of a water valve or level instrument failure in relation to the fresh brine tank.
- the fresh brine volume required for a Rl 200 tank based on 0.4 Bed Volumes of fresh brine required is 350L.
- the fresh brine volume requirement is 10OL.
- These small volumes can be added by first adding the water volume based on level rise in the tank followed by the saturated brine volume based on level rise in the tank.
- the regenerant tank receives the regenerant from the regeneration vessel 324 and 326 (and any additional vessels such as 328) and will supply regenerant by gravity back to the regeneration vessels. - 50 -
- the quality of the regenerant in the tank is monitored by the use of a conductivity probe fitted to the tank.
- the size of the regenerant tank will depend on the volume of the regeneration vessels. Conveniently volume of the tank is around 10% of the total daily turnover. In an arrangement the tank may be have an internal fresh brine tank.
- regenerant tank will operate at a top fluid level.
- resin is collected from an underflow settler 305.
- the resin is transported via pipe 306 to the splitter box 308 where a portion of the flow (approximately 10%) is passes into the concentrator 300 via pipe 312.
- the remainder of the flow is returned via pipe 310 to the contactors 302.
- the overflow from the concentrator is also returned to the contactors 302 by pipe 313.
- Concentrated resin is transferred from the bottom of concentrator to an empty regeneration vessel 324 or 326, in response to a signal from a sensor associated with the vessel.
- the resin is transferred via pipe 318 to a common manifold 370 connected to all vessels. - 55 -
- Control valves operate in response the vessel sensors to allow the resin to pass into an empty vessel.
- the resin is then subjected to the regeneration process as earlier described. Excess water is first drained from the vessel and is returned to the contactors via the fresh resin manifold 344.
- the vacuum pump associated with the vessel 330, 332 will quickly drain the excess water.
- Regenerant (brine) is then added to the vessel from the regenerant tank 360 via the regenerant manifold 372.
- the regenerant is drained off by the associated vacuum pump.
- the first fraction (approximately 0.3 bed volumes) containing the highest concentration of DOC is sent to the waste drain 374 via the waste drain manifold 376.
- the remainder is returned to the regenerant tank via the brine drain manifold 378.
- a concentrated solution of brine is added the vessel in a plug flow manner.
- This brine is obtained from the fresh brine tank 350 via the fresh brine manifold 380 and may be a saturated brine solution or may have been further diluted.
- This solution is followed by fresh water 381 piped into the vessel via the fresh water manifold 382. The fresh water is used to rinse the resin.
- the concentrated solution of brine is drained off by the vacuum pump associated with the vessel. This solution is also sent to the fresh brine tank 350 via the fresh brine manifold.
- a conductivity sensor detects when fresh water is being pumped from the vessel. Once the sensor detects the fresh water the resin is pumped from the vessel to the fresh resin tank 320 via the fresh resin pumps 340 and the fresh resin manifold 344.
- the stirrer 384 may be used to fluidise the resin to facilitate the transfer of the resin from the vessel to the tank. - 56 -
- the vacuum pump operates continuously as resin is added to the vessel, firstly drawing off water, then regenerant (the first fraction being sent to waste), then concentrated regenerant and finally the rinse water.
- the regeneration system has a constant regenerant / DOC waste discharge in each regeneration.
- more conventional designs use a brine / DOC waste purge every use and a whole discharge after a number of uses (eg. after 10 regenerations).
- BV bed volumes
- the expected waste volume figure is 414 gal / MG. This assumes the regenerant is discharged after ten uses.
- the present invention effectively does not generate a rinse water waste volume. - 59 -
- Mean relates to the mean particle sizes of the resin beads - 61 -
- the cycled resin was examined under a microscopy and very fine non-resin particles with a few fine beads were observed. It is suspected that these impurities were introduced from the brine. It was also possible that this was emulsion polymer cleaned from the pores of the resin.
- IBV of resin was removed from tank 214 by mixing into a homogenous solution and pumping into column 210. At the same time the drain was left open and the brine is drained and collected before being returned to tank 214. Pulling the brine through the bed effectively acted as an extra regeneration step. Resin from column 210 is then transferred to tank 214 with the remaining brine by opening drain point and allowing the resin to slide out (shown by flow line 224). 0.4BV of fresh brine with a salt concentration of 120g/L is added to column 212. This is pumped out of the column at 116ml/min and sent to tank 214 (shown by flow line
- This arrangement reduces the need to use sensors or flow controllers when concentrating resin for subsequent regeneration.
- the suitable transfer tank is a Im by Im square section tank with a 70° internal angle hopper base.
- the overall height of the transfer tank is governed by the height of the contactors.
- An alternative tested transfer tank was circular with a 90° internal angle base cone. The diameter can be reduced to 600mm (a pipe section) in smaller water plants if required, and additional transfer tanks of the same type can be added for larger systems.
- the splitter box 308 is an open channel with an adjustable "gate" (not shown) set to divert a portion of the recycle flow to the transfer tank.
- the splitter box can be located to the side of the transfer tank at enough height to allow resin slurry to flow into the transfer tank 300.
- the regenerated (fresh) resin is pumped along the regenerated resin return pipe 318 into a fresh resin storage tank 320.
- the fresh resin storage tank is used to provide a buffer for the addition of fresh resin.
- Regenerated resin is pumped from the regeneration tanks to the fresh resin tank which is sized to hold at least a single batch of fresh resin (one regeneration tank volume).
- the use of a hopper style tank allows the entire contents to be discharged without the need for a mixer.
- a continuous water bleed can be passed through the fresh resin pumps which will act as a water flush for the fresh resin hopper, and should avoid system blockages.
- Rl 200 dimensions are 1200 mm by 1200mm by 1800mm tall
- the resin volumes are based on a resin concentration of 20ml/L and a regeneration rate of 5%.
- a 5MGD plant at 20 ml/L and 5% regeneration rate could use 12 R600 model tanks or 3 Rl 200 tanks.
- the regenerant system includes a salt saturator with a saturated brine pump (not depicted) which supplies saturated brine to a fresh brine tank 350.
- the fresh brine tank is a small - 51 -
- the system is equipped with two resin pumps (depicted as the single pump 340) to allow the process to continue operating at a reduced transfer rate in the event of a pump failure.
- Each pump should have its own discharge line (depicted as the single pipe 342) to avoid one pump from being able to "overpower" the other.
- Each pump handles 50% of the system capacity.
- the fresh resin pumps are connected to a common resin discharge pipe 344 from the regeneration tanks.
- the system is envisaged to operate with only a single tank to be discharging at one time.
- the resin transfer time may be 10 minutes out of an estimated total cycle time of approximately 200 minutes. This avoids the need to provide multiple designs to cater for a range of flows. It is believed that this arrangement will not significantly increase overall cycle times as resin transfer is a small fraction of the total regeneration cycle time. Of course the size of the discharge could be increased if it is expected to have multiple tanks discharging resin at the same time.
- the discharge pipe is continuously flushed with a low volumetric rate of water (eg 10-20 % of full pump flow). This allows the pumps to operate continuously with no frequent starts, should ensure that resin does not form blockages in the transfer pipes during down time and flushes the base of the fresh resin tank which should prevent blockages in that tank.
- a low volumetric rate of water eg 10-20 % of full pump flow
- the water flush supply is supplied from a common water system with a pressure regulator and manual valve to adjust the flow rate.
- the suction pipe has a flow switch and / or flow meter to warn the operator of a water supply failure.
- the common regenerant drain discharge manifold should be sized to cope with 50% of the tanks using the common outlet at any one time. This assumes a regeneration tank will be draining regenerant for approximately 50% of the total regeneration cycle time.
- Regeneration vessel 328 is an example of an additional vessel when connected to the existing manifold. The interval between fresh resin transfers to the fresh resin tank will decrease as the number of regeneration vessels connected to the manifold is increased.
- the present invention is also expected to reduce salt consumption.
- the regeneration system expected salt consumption may be in the range of 150 to 300 lb/MG.
- the expected salt consumption figure is 500 to 900 Ib/MG. This assumes ten (10) brine uses and excludes salt that could be recovered from brine treatment.
- a 12% brine solution has been successfully used to regenerate MIEX® resin, when in service in water treatment plants. This concentration has been found to be safe, as it did not cause osmotic shock to the resin beads. However, replenishment of resin is still required on these plants due to losses by chemical and physical attrition and by losing intact beads over the settler.
- the resin was subjected to an attrition test to simulate ordinary wear and tear during use in a water treatment plant.
- PSD particle size distribution
- the particle size distribution (PSD) was measured using a Coulter L230 and the mean particle diameter was recorded.
- the resin (20 ml) was rinsed into a 250 ml PVC bottle and 10 g of glass beads (2-3 mm in diameter was added.
- the resin was mashed with the glass beads in the bottle for 60 minutes on a shaker table (speed was 1 Hz, average displacement was 6 cm) and analysed to measure the reduction in particle size.
- Particle size distribution and microscopic observations were performed to determine resin attrition and to observe presence of apparent cracks/crazing on bead surfaces respectively.
- the information generated by particle size analysis for the virgin resin and cycled resin are given in Tables 7a-7d below.
- Tables 7a to 7d Resin bead size distribution statistics of virgin resin after 665 regenerations of virgin resin including attrition results. - 60 -
- Fig 21 provides a comparison after attrition between virgin resin and cycled virgin resin which was subjected to saturated brine.
- FIGS. 22 and 23 depict a pair of photographs of the virgin resin (fig 22) and cycled resins (fig 23).
- the shape of the resin varies from small to large and spherical to elongated types. Small cavities on the surface of beads can be seen in both cases.
- the surface morphology shown below did not indicate any difference between the samples. Also, observations did not reveal any increase in number of smaller sized resin beads.
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Abstract
Description
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Application Number | Priority Date | Filing Date | Title |
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AU2004904207A AU2004904207A0 (en) | 2004-07-28 | Plug-Flow Regeneration Process | |
US68357105P | 2005-05-23 | 2005-05-23 | |
PCT/AU2005/001111 WO2006010216A1 (en) | 2004-07-28 | 2005-07-28 | Plug-flow regeneration process |
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EP1776190A1 true EP1776190A1 (en) | 2007-04-25 |
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Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090242487A1 (en) | 2004-12-15 | 2009-10-01 | Orica Australia Pty Ltd | Magnetic particle removal process |
KR100735707B1 (en) * | 2006-09-29 | 2007-07-06 | 엘지전자 주식회사 | Laundry dryer and method for controlling the same |
BR112012004979A8 (en) | 2009-09-03 | 2017-03-21 | Fbsciences Holdings Inc | COMPOSITIONS FOR SEED TREATMENT AND METHODS |
US20110077155A1 (en) * | 2009-09-28 | 2011-03-31 | Goodwin Brian B | Fertilizer compositions and methods |
FR2954174B1 (en) * | 2009-12-17 | 2014-04-11 | Otvs A | PROCESS FOR POTABILIZING AND / OR PURIFYING WATER COMPRISING THE REMOVAL OF A TARGET COMPOUND AND FILTRATION WITHIN A FILTER DRUM |
WO2012009641A2 (en) | 2010-07-15 | 2012-01-19 | Fbsciences Holdings, Inc. | Microorganism compositions and methods |
US9180411B2 (en) | 2011-09-22 | 2015-11-10 | Chevron U.S.A. Inc. | Apparatus and process for treatment of water |
GB201121950D0 (en) * | 2011-12-19 | 2012-02-01 | T & L Process Technology Ltd | Treatment process |
US10448635B2 (en) | 2012-01-12 | 2019-10-22 | Fbsciences Holdings, Inc. | Modulation of plant biology |
NL2008808C2 (en) * | 2012-05-14 | 2013-11-18 | Pwn Technologies B V | ION EXCHANGE PROCESS WITH PLUG FLOW CONDITIONS AND SHORT RESIDENCE TIMES. |
US10131552B2 (en) * | 2015-01-06 | 2018-11-20 | Amperage Energy Inc. | Ion exchange system for removing sulfate ions from water |
US20180148348A1 (en) * | 2015-05-08 | 2018-05-31 | Dow Global Technologies Llc | Process of use of adsorbent resin particles |
CA3052685C (en) * | 2017-02-10 | 2023-12-05 | Outotec (Finland) Oy | Method and arrangement for controlling a dewatering process |
CN106881159B (en) * | 2017-03-23 | 2018-08-24 | 南京大学 | A kind of ion exchange resin fixed bed counter-current regeneration device and its application method |
US11028124B2 (en) * | 2018-05-07 | 2021-06-08 | Repligen Corporation | Methods, devices and systems for 3-stage filtration |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2060430A (en) * | 1979-10-13 | 1981-05-07 | Invergordon Distillers Ltd | Regeneration of ion exchange resins |
WO1996007615A1 (en) * | 1994-09-09 | 1996-03-14 | South Australian Water Corporation | Water treatment process |
EP1431248A2 (en) * | 2002-12-18 | 2004-06-23 | Rohm And Haas Company | Water treatment system with low waste volume |
WO2005105677A1 (en) * | 2004-04-30 | 2005-11-10 | Orica Australia Pty Ltd | Regeneration process |
WO2006029478A2 (en) * | 2004-09-17 | 2006-03-23 | Orica Australia Pty Ltd | Effluent treatment process |
Family Cites Families (118)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1190863A (en) | 1916-01-26 | 1916-07-11 | Charles Louis Corne | Settling-tank. |
US2642514A (en) | 1946-08-10 | 1953-06-16 | American Cyanamid Co | Ion exchange process with magnetic ion exchange resins |
US2697724A (en) | 1950-03-15 | 1954-12-21 | Sharples Corp | Ion exchange |
AU435693B2 (en) | 1967-04-20 | 1973-05-14 | Ion-exchange adsorbents and process involving same | |
US3996131A (en) | 1971-06-16 | 1976-12-07 | Universal Oil Products Company | Precoat for permeability separation systems |
US3808305A (en) | 1971-07-27 | 1974-04-30 | H Gregor | Crosslinked,interpolymer fixed-charge membranes |
US4154675A (en) | 1972-06-02 | 1979-05-15 | Viscose Group Limited | Ion exchange processes using cellulosic materials |
US4049546A (en) | 1974-11-11 | 1977-09-20 | Rohm And Haas Company | Decolorization of effluents from pulp mills |
JPS5199853A (en) | 1975-02-28 | 1976-09-03 | Hitachi Ltd | |
GB1559809A (en) | 1976-02-28 | 1980-01-30 | Northern Eng Ind | Method of and apparatus for effecting interaction between liquid and solid |
US4123396A (en) | 1976-08-27 | 1978-10-31 | California Institute Of Technology | Impregnated metal-polymeric functional beads |
US4956061A (en) | 1977-12-09 | 1990-09-11 | Oronzio De Nora Permelec S.P.A. | Production of halogens by electrolysis of alkali metal halides in an electrolysis cell having catalytic electrodes bonded to the surface of a solid polymer electrolyte membrane |
US4207397A (en) | 1978-09-15 | 1980-06-10 | Water Refining Company, Inc. | Method for recovering and treating brine from water softener regeneration |
US4312956A (en) | 1978-09-19 | 1982-01-26 | Rohm And Haas Company | Filtration and deionization prepared from cationic and anionic emulsion ion exchange resins |
US4314905A (en) | 1978-11-02 | 1982-02-09 | Purdue Research Foundation | Columnar fine mesh magnetized ion exchange resin system |
US4269760A (en) | 1978-11-09 | 1981-05-26 | Sinloihi Company Limited | Fine spherical polymer particles containing inorganic pigment and/or coloring agent and process for the preparation thereof |
DE2947765C2 (en) | 1978-11-28 | 1985-09-19 | Koei Chemical Co., Ltd., Osaka | Process for the production of phenols from aqueous solutions |
AU534146B2 (en) | 1978-12-01 | 1984-01-05 | Commonwealth Scientific And Industrial Research Organisation | Continuous countercurrent solid/liquid contact apparatus and method |
AU534337B2 (en) | 1979-06-08 | 1984-01-19 | Commonwealth Scientific And Industrial Research Organisation | Process for composite polymer beads |
US4279755A (en) | 1980-02-26 | 1981-07-21 | Alexander Himsley | Continuous countercurrent ion exchange process |
US4289617A (en) | 1980-05-05 | 1981-09-15 | Water Refining Company, Inc. | Water softening and reverse osmosis system |
US4473474A (en) | 1980-10-27 | 1984-09-25 | Amf Inc. | Charge modified microporous membrane, process for charge modifying said membrane and process for filtration of fluid |
US4673504A (en) | 1980-10-27 | 1987-06-16 | Cuno Inc. | Charge modified microporous membrane |
US4447475A (en) | 1980-12-03 | 1984-05-08 | Ici Australia Limited | Process for composite polymer beads |
US4329225A (en) | 1980-12-29 | 1982-05-11 | Water Refining Company, Inc. | Mixed bed deionizer |
US4385993A (en) * | 1981-06-22 | 1983-05-31 | American Petro Mart, Inc. | Method and apparatus for folded moving bed ion exchange system |
US4537683A (en) | 1982-02-01 | 1985-08-27 | Rohm And Haas Company | Trihalomethane precursor removal using ion exchange emulsions |
US4702840A (en) | 1982-02-05 | 1987-10-27 | Pall Corporation | Charge modified polyamide membrane |
US4935450A (en) | 1982-09-17 | 1990-06-19 | Therapeutical Systems Corporation | Cancer therapy system for effecting oncolysis of malignant neoplasms |
AU2398984A (en) | 1983-02-22 | 1984-08-30 | Schubring, R.W. | Alkaline waste water treatment and separating apparatus |
US4724082A (en) | 1984-04-19 | 1988-02-09 | The Dow Chemical Company | Ion exchange process having increased flow rates |
DE3568946D1 (en) | 1984-07-09 | 1989-04-27 | Millipore Corp | Improved electrodeionization apparatus and method |
US4804465A (en) | 1984-09-04 | 1989-02-14 | Kinetico, Inc. | Water treatment apparatus |
US4648976A (en) | 1985-03-07 | 1987-03-10 | Belco Pollution Control Corporation | Integral water demineralizer system and method |
US4737921A (en) | 1985-06-03 | 1988-04-12 | Dynamic Digital Displays, Inc. | Three dimensional medical image display system |
US4693832A (en) | 1985-11-27 | 1987-09-15 | Quantum Technologies, Inc. | Preparation of safe drinking water |
US4670154A (en) | 1985-12-02 | 1987-06-02 | Uip Engineered Products Corporation | Mixed resin bed deionizer |
JPH0644074B2 (en) | 1986-02-18 | 1994-06-08 | 動力炉・核燃料開発事業団 | Treatment method for wastewater containing uranium and fluorine |
US4734200A (en) | 1986-04-04 | 1988-03-29 | Advanced Separation Technologies Incorporated | Process for removal of fluoride and phosphorus-type contaminants from acidic wastewater |
DE3623796A1 (en) | 1986-07-15 | 1988-01-28 | Dow Chemical Rheinwerk Gmbh | DEVICE AND ADSORPTION METHOD FOR THE SELECTIVE REMOVAL OF IONS FROM LIQUIDS |
DE3710804A1 (en) | 1987-03-31 | 1988-10-20 | Basf Ag | METHOD FOR THE CLEANING AND DISPOSAL OF SOOT AND ASHYWOOD |
US4839057A (en) | 1987-09-30 | 1989-06-13 | Alar Engineering Corporation | Water treatment system |
US4952386A (en) | 1988-05-20 | 1990-08-28 | Athens Corporation | Method and apparatus for purifying hydrogen fluoride |
US6020210A (en) | 1988-12-28 | 2000-02-01 | Miltenvi Biotech Gmbh | Methods and materials for high gradient magnetic separation of biological materials |
JPH0753276B2 (en) | 1989-10-03 | 1995-06-07 | 栗田工業株式会社 | Fluoride-containing water treatment method |
DE3938245A1 (en) | 1989-11-17 | 1991-05-23 | Erwin Lotze | Liq. filtration by fine mobile magnetic particles layer - subject to variable field and periodically transformed for regeneration |
FR2657076B1 (en) | 1990-01-15 | 1992-09-04 | Inst Textile De France | USE OF GRAFT CELLULOSE FOR THE PURIFICATION OF WATER. |
IT1239015B (en) * | 1990-01-24 | 1993-09-20 | Valerio Mancini | METHOD FOR THE USE AND REGENERATION OF ANIONIC RESINS IN DYEING AND SIMILAR WASTEWATER SYSTEMS. |
US5215632A (en) | 1990-04-30 | 1993-06-01 | Occidental Chemical Corporation | Fluoride removal from aqueous streams |
US5120688A (en) | 1990-05-29 | 1992-06-09 | The Morgan Crucible Company Plc | Pressureless sintered silicon nitride-boron nitride composite |
US5236595A (en) | 1990-07-06 | 1993-08-17 | International Environmental Systems, Inc., Usa | Method and apparatus for filtration with plural ultraviolet treatment stages |
US5248424A (en) | 1990-08-17 | 1993-09-28 | Zenon Environmental Inc. | Frameless array of hollow fiber membranes and method of maintaining clean fiber surfaces while filtering a substrate to withdraw a permeate |
US5149437A (en) | 1991-03-29 | 1992-09-22 | Wilkinson Theodore L | Water filter |
US5143583A (en) | 1991-04-02 | 1992-09-01 | Marchessault Robert H | Preparation and synthesis of magnetic fibers |
US5128041A (en) | 1991-05-15 | 1992-07-07 | Pall Corporation | Microporous membrane, method of manufacture, and method of use |
GB9115018D0 (en) | 1991-07-11 | 1991-08-28 | Bradtec Ltd | Purification of solutions |
JP2697399B2 (en) | 1991-09-13 | 1998-01-14 | 三菱電機株式会社 | Positioning device and program display method thereof |
US5182023A (en) | 1991-10-17 | 1993-01-26 | Texas Romec, Inc. | Process for removing arsenic from water |
SE469031B (en) | 1991-10-31 | 1993-05-03 | Electrolux Ab | DEVICE FOR WATER PURIFICATION MEDIUM REVERSE OSMOS |
US5403495A (en) | 1992-03-13 | 1995-04-04 | Tetra Technologies, Inc. | Fluoride removal system |
US5728302A (en) | 1992-04-09 | 1998-03-17 | Groundwater Services, Inc. | Methods for the removal of contaminants from subterranean fluids |
FR2696440B1 (en) | 1992-10-02 | 1995-02-10 | Dumez Lyonnaise Eaux | Method and installation for treating liquid effluents containing in particular pollutants in solution by membrane and gravity separations. |
PT604095E (en) | 1992-12-23 | 2001-10-31 | Imerys Minerals Ltd | PROCESS FOR THE TREATMENT OF SUSPENSIONS OF RESIDUAL MATERIAL |
JP2947314B2 (en) | 1992-12-24 | 1999-09-13 | 株式会社クボタ | Adsorption and reaction equipment |
US5254257A (en) | 1993-01-19 | 1993-10-19 | Culligan International Company | Reclaiming of spent brine |
US5415765A (en) | 1993-04-07 | 1995-05-16 | Kinetico Engineered Systems, Inc. | Water treatment system |
US5595666A (en) | 1993-05-07 | 1997-01-21 | The United States Of America As Represented By The United States Department Of Energy | Removal of radioactive materials and heavy metals from water using magnetic resin |
US5320756A (en) | 1993-06-29 | 1994-06-14 | Church & Dwight Co., Inc. | Method of treating aqueous alkaline effluents derived from cleaning electronic circuit assemblies |
US5449522A (en) | 1993-08-24 | 1995-09-12 | Hill; Albert F. | Pharmaceutical composition for immunoenhancement therapy |
US5840770A (en) | 1993-08-24 | 1998-11-24 | Hill Medical Corporation | Method of killing tumor cells |
US5464530A (en) | 1993-12-08 | 1995-11-07 | Stivers; Lewis E. | Ion exchange methods and systems incorporating regenerant recycling |
US6110375A (en) | 1994-01-11 | 2000-08-29 | Millipore Corporation | Process for purifying water |
US5855790A (en) | 1994-02-07 | 1999-01-05 | Selective Environmental Technologies, Inc. | Magnetic particles, a method for the preparation thereof and their use in the purification of solutions |
US5547585A (en) | 1994-03-28 | 1996-08-20 | Shepherd; Samuel L. | Process for the removal of contaminants from a fluid stream |
AU749656B2 (en) | 1994-09-09 | 2002-06-27 | Orica Australia Pty Ltd | Water treatment process |
AUPM959994A0 (en) | 1994-11-22 | 1994-12-15 | Ici Australia Operations Proprietary Limited | Water treatment process |
AU744706B2 (en) | 1994-09-09 | 2002-02-28 | Chemicals Australia Operations Pty Ltd | Polymer beads and method for preparation thereof |
AUPM807094A0 (en) | 1994-09-09 | 1994-10-06 | Commonwealth Scientific And Industrial Research Organisation | Polymer beads and method for preparation thereof |
US5494582A (en) | 1995-03-01 | 1996-02-27 | Nalco Chemical Company | Removal of selenium from water by ion-exchange |
US5932099A (en) | 1995-07-25 | 1999-08-03 | Omnium De Traitements Et De Valorisation (Otv) | Installation for biological water treatment for the production of drinkable water |
JP3244404B2 (en) | 1995-08-16 | 2002-01-07 | シャープ株式会社 | Water treatment method and water treatment device |
FR2746788B1 (en) | 1996-04-02 | 1998-06-05 | Degremont | DOUBLE FLOW FILTER FOR BIOLOGICAL PURIFICATION OF EFFLUENTS |
WO1998001208A1 (en) | 1996-07-08 | 1998-01-15 | Memtec America Corporation | Cationically charge-modified membranes |
US5876685A (en) | 1996-09-11 | 1999-03-02 | Ipec Clean, Inc. | Separation and purification of fluoride from industrial wastes |
CA2186963C (en) | 1996-10-01 | 1999-03-30 | Riad A. Al-Samadi | High water recovery membrane purification process |
US6464881B2 (en) | 1996-10-21 | 2002-10-15 | Orelis | Inorganic nanofiltration membrane and its application in the sugar industry |
US6120688A (en) | 1997-02-25 | 2000-09-19 | Zenon Environmental, Inc. | Portable reverse osmosis unit for producing drinking water |
US6027649A (en) | 1997-04-14 | 2000-02-22 | Zenon Environmental, Inc. | Process for purifying water using fine floc and microfiltration in a single tank reactor |
FR2771727B1 (en) | 1997-11-28 | 2000-02-11 | Sgs Thomson Microelectronics | DEFLUORURATION OF WASTEWATER |
JP3169899B2 (en) | 1998-07-15 | 2001-05-28 | 日本電気環境エンジニアリング株式会社 | Method and apparatus for treating fluorine-containing wastewater |
WO2000030742A1 (en) | 1998-11-23 | 2000-06-02 | Zenon Environmental Inc. | Water filtration using immersed membranes |
US6200471B1 (en) | 1999-01-12 | 2001-03-13 | Innova Pure Water, Inc. | Bottle specialty water filters |
US6491827B1 (en) | 1999-02-12 | 2002-12-10 | Steen Research, Llc | Process for reducing true color in waste liquids |
US6355221B1 (en) | 1999-04-05 | 2002-03-12 | Bp Corporation North America Inc. | Process for removing soluble fluoride from a waste solution containing the same |
US6776913B1 (en) | 1999-07-20 | 2004-08-17 | Juzer Jangbarwala | Water softening method and apparatus for use therewith |
US6338803B1 (en) | 1999-08-30 | 2002-01-15 | Koch Microelectronic Service Co., Inc. | Process for treating waste water containing hydrofluoric acid and mixed acid etchant waste |
US6416668B1 (en) | 1999-09-01 | 2002-07-09 | Riad A. Al-Samadi | Water treatment process for membranes |
US6197193B1 (en) | 1999-10-21 | 2001-03-06 | Virgil L. Archer | Drinking water filter |
US6203705B1 (en) | 1999-10-22 | 2001-03-20 | Koch Microelectronic Service Company, Inc. | Process for treating waste water containing copper |
US6613232B2 (en) | 2000-03-21 | 2003-09-02 | Warren Howard Chesner | Mobile floating water treatment vessel |
US6824685B2 (en) | 2000-03-27 | 2004-11-30 | Ebara Corporation | Method and apparatus for treating waste water |
DE10033583A1 (en) | 2000-07-11 | 2002-01-24 | Bayer Ag | Superparamagnetic polymer beads |
US6517723B1 (en) | 2000-07-27 | 2003-02-11 | Ch2M Hill, Inc. | Method and apparatus for treating wastewater using membrane filters |
JP4734579B2 (en) | 2000-08-10 | 2011-07-27 | Jnc株式会社 | Difluoromethyl ether derivative and process for producing the same |
US6372143B1 (en) | 2000-09-26 | 2002-04-16 | Hydrometrics, Inc. | Purification of produced water from coal seam natural gas wells using ion exchange and reverse osmosis |
US7025884B2 (en) | 2000-11-10 | 2006-04-11 | Ch2M Hill, Inc. | Method and apparatus for treatment of a fluid system |
AU1780402A (en) | 2000-11-10 | 2002-05-21 | Ch2M Hill Inc | Method and apparatus for treatment of drinking water |
US7028009B2 (en) | 2001-01-17 | 2006-04-11 | Contentguardiholdings, Inc. | Method and apparatus for distributing enforceable property rights |
AUPR604001A0 (en) | 2001-06-29 | 2001-07-26 | Orica Australia Pty Ltd | Vesiculated polyester granules |
US6723245B1 (en) | 2002-01-04 | 2004-04-20 | Nalco Company | Method of using water soluble cationic polymers in membrane biological reactors |
AUPR987802A0 (en) | 2002-01-08 | 2002-01-31 | Commonwealth Scientific And Industrial Research Organisation | Complexing resins and method for preparation thereof |
WO2003082748A1 (en) * | 2002-04-03 | 2003-10-09 | Orica Australia Pty Ltd | Process for regenerating ion-exchange resins |
TW593167B (en) | 2002-10-25 | 2004-06-21 | Ind Tech Res Inst | Method for treating wastewater/water with membrane bioreactor |
WO2004098776A1 (en) * | 2003-05-09 | 2004-11-18 | Clean Teq Pty Ltd | Method and apparatus for desorbing material |
GB0311153D0 (en) * | 2003-05-15 | 2003-06-18 | Otv Sa | Ion-exchange process |
US6998054B2 (en) | 2003-12-31 | 2006-02-14 | The Boc Group, Inc. | Selective fluoride and ammonia removal by chromatographic separation of wastewater |
DE102004016625A1 (en) | 2004-04-05 | 2005-10-20 | Pmdtechnologies Gmbh | PMD system and method of operating the same |
US7291272B2 (en) | 2004-05-07 | 2007-11-06 | Orica Australia Pty Ltd. | Inorganic contaminant removal from water |
-
2005
- 2005-07-28 AU AU2005266851A patent/AU2005266851B2/en active Active
- 2005-07-28 WO PCT/AU2005/001111 patent/WO2006010216A1/en active Application Filing
- 2005-07-28 US US11/572,905 patent/US7763666B2/en active Active
- 2005-07-28 EP EP05764193.8A patent/EP1776190B1/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2060430A (en) * | 1979-10-13 | 1981-05-07 | Invergordon Distillers Ltd | Regeneration of ion exchange resins |
WO1996007615A1 (en) * | 1994-09-09 | 1996-03-14 | South Australian Water Corporation | Water treatment process |
US20040050785A1 (en) * | 1994-09-09 | 2004-03-18 | Nguyen Hung Van | Water treatment process |
EP1431248A2 (en) * | 2002-12-18 | 2004-06-23 | Rohm And Haas Company | Water treatment system with low waste volume |
WO2005105677A1 (en) * | 2004-04-30 | 2005-11-10 | Orica Australia Pty Ltd | Regeneration process |
WO2006029478A2 (en) * | 2004-09-17 | 2006-03-23 | Orica Australia Pty Ltd | Effluent treatment process |
Non-Patent Citations (2)
Title |
---|
R. LANGE ET AL: "Design and construction of the world's first large scale MIEX water treatment plant" MIEX RESOURCES PUBLISHED PAPERS, [Online] 2001, XP002481155 Australia Retrieved from the Internet: URL:http://www.miexresin.com/files/publishedPapers/WanAUSAWAFC01.pdf> [retrieved on 2008-04-19] * |
See also references of WO2006010216A1 * |
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US7763666B2 (en) | 2010-07-27 |
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